HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.48560/rspo.13388 |
Resumo: | ABSTRACT PURPOSE To report the visual outcomes of non-arteritic CRAO (NA-CRAO) patients submitted to hyperbaric oxygen therapy (HBOT) in our hospital. METHODS Retrospective anaylsis of patients with CRAO submitted to HBOT between 2010 and 2017. Only patients with non-transient NA-CRAO, absence of a patent cilioretinal artery and less of 24 hours of evolution were included. All patients were submitted to sessions of 90 minutes lenght with 100% oxygen at 2,4atm. Primary outcome was visual acuity change (logMar) pre and post treatment. Adverse effects from the treatment were registered. RESULTS Overall fourteen patients met the inclusion criteria, 57% males (n=8) and 43% females (n=6), with a median age of 68 years (min.41; max.92). VA at baseline was count-fingers (CF) or worse in 85,7% (n=12) of the patients. The median time between the symptoms onset and the beginning of the treatment was 7.0 hours (min.2; max.24h). The baseline and post treatment best-corrected visual acuity (BCVA) were 2,34±1,16 and 1,39±0,94 logMar respectively, which was statistical significant (p=0,007). VA gain was greater than 0.3 logMar in 71,4% of the patients. No serious adverse effects from HBOT were registered. One patient experienced mild ear barotrauma. CONCLUSIONS Patients with NA-CRAO experienced VA improvement after HBOT, although with important limitations. The implementation of strategies to reduce the time between the onset of symptoms and treatment could result in a higher functional gain. |
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HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCEArtigos OriginaisABSTRACT PURPOSE To report the visual outcomes of non-arteritic CRAO (NA-CRAO) patients submitted to hyperbaric oxygen therapy (HBOT) in our hospital. METHODS Retrospective anaylsis of patients with CRAO submitted to HBOT between 2010 and 2017. Only patients with non-transient NA-CRAO, absence of a patent cilioretinal artery and less of 24 hours of evolution were included. All patients were submitted to sessions of 90 minutes lenght with 100% oxygen at 2,4atm. Primary outcome was visual acuity change (logMar) pre and post treatment. Adverse effects from the treatment were registered. RESULTS Overall fourteen patients met the inclusion criteria, 57% males (n=8) and 43% females (n=6), with a median age of 68 years (min.41; max.92). VA at baseline was count-fingers (CF) or worse in 85,7% (n=12) of the patients. The median time between the symptoms onset and the beginning of the treatment was 7.0 hours (min.2; max.24h). The baseline and post treatment best-corrected visual acuity (BCVA) were 2,34±1,16 and 1,39±0,94 logMar respectively, which was statistical significant (p=0,007). VA gain was greater than 0.3 logMar in 71,4% of the patients. No serious adverse effects from HBOT were registered. One patient experienced mild ear barotrauma. CONCLUSIONS Patients with NA-CRAO experienced VA improvement after HBOT, although with important limitations. The implementation of strategies to reduce the time between the onset of symptoms and treatment could result in a higher functional gain.Ajnet2018-05-09T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.48560/rspo.13388eng1646-69501646-6950Coelho, Pedro Aguiarinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-22T17:06:04Zoai:ojs.revistas.rcaap.pt:article/13388Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:01:41.011369Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
title |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
spellingShingle |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE Coelho, Pedro Aguiar Artigos Originais |
title_short |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
title_full |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
title_fullStr |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
title_full_unstemmed |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
title_sort |
HYPERBARIC OXYGEN IN CRAO – OUR EXPERIENCE |
author |
Coelho, Pedro Aguiar |
author_facet |
Coelho, Pedro Aguiar |
author_role |
author |
dc.contributor.author.fl_str_mv |
Coelho, Pedro Aguiar |
dc.subject.por.fl_str_mv |
Artigos Originais |
topic |
Artigos Originais |
description |
ABSTRACT PURPOSE To report the visual outcomes of non-arteritic CRAO (NA-CRAO) patients submitted to hyperbaric oxygen therapy (HBOT) in our hospital. METHODS Retrospective anaylsis of patients with CRAO submitted to HBOT between 2010 and 2017. Only patients with non-transient NA-CRAO, absence of a patent cilioretinal artery and less of 24 hours of evolution were included. All patients were submitted to sessions of 90 minutes lenght with 100% oxygen at 2,4atm. Primary outcome was visual acuity change (logMar) pre and post treatment. Adverse effects from the treatment were registered. RESULTS Overall fourteen patients met the inclusion criteria, 57% males (n=8) and 43% females (n=6), with a median age of 68 years (min.41; max.92). VA at baseline was count-fingers (CF) or worse in 85,7% (n=12) of the patients. The median time between the symptoms onset and the beginning of the treatment was 7.0 hours (min.2; max.24h). The baseline and post treatment best-corrected visual acuity (BCVA) were 2,34±1,16 and 1,39±0,94 logMar respectively, which was statistical significant (p=0,007). VA gain was greater than 0.3 logMar in 71,4% of the patients. No serious adverse effects from HBOT were registered. One patient experienced mild ear barotrauma. CONCLUSIONS Patients with NA-CRAO experienced VA improvement after HBOT, although with important limitations. The implementation of strategies to reduce the time between the onset of symptoms and treatment could result in a higher functional gain. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-05-09T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.48560/rspo.13388 |
url |
https://doi.org/10.48560/rspo.13388 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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1646-6950 1646-6950 |
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info:eu-repo/semantics/openAccess |
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openAccess |
dc.publisher.none.fl_str_mv |
Ajnet |
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Ajnet |
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reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799130481911922688 |